Furosemide
- Product NDC
- 73542-102
- 11-digit product format
- 735420102
- Labeler code
- 73542
- Product ID
- 73542-102_dddc74d0-e63a-431b-a222-12c45bdc0c16
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Furosemide
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Maiva Pharma Private Limited
- Application
- ANDA203428
- Marketing category
- ANDA
- Marketing start
- 2025-06-16
- Substance
- FUROSEMIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Furosemide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FUROSEMIDE | 10 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7LXU5N7ZO5 |
| Rxcui | 1719286, 1719290, 1719291 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73542-102-25 | Furosemide | 25 in 1 CARTON | INJECTION | 25 | | 1 |
| 73542-102-25 | Furosemide | 4 mL in 1 VIAL | INJECTION | 4 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73542-102-25 | 73542010225 | 25 VIAL in 1 CARTON (73542-102-25) / 4 mL in 1 VIAL | 25 vial | 2025-06-16 | No | No | Current |